Reaktion #82546

ord-f7e0132fef5c4ba29f07494aaaf13849

Reaktionsgleichung

Cc1nc(N)nc(N)c1I
2,4-diamino-5-iodo-6-methylpyrimidine
CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[C](F)=CC(C)(C)c1ccc(Cl)cc1
1-fluoro-3-(4-chlorophenyl)-3-methyl-1-tributylstannyl-1-butene
c1coc(P(c2ccco2)c2ccco2)c1
tri-2-furylphosphine
Cc1nc(N)nc(N)c1C(F)=CC(C)(C)c1ccc(Cl)cc1
2,4-diamino-6-methyl-5-[1-fluoro-3-methyl-3-(4-chlorophenyl)-1-butenyl]pyrimidine

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThis compound is prepared in a manner analogous to that of Step E of Example 4

Vorschrift

This compound is prepared in a manner analogous to that of Step E of Example 4, using 1.2 grams (0.0048 mole) of 2,4-diamino-5-iodo-6-methylpyrimidine, 2.3 grams (0.0048 mole) of 1-fluoro-3-(4-chlorophenyl)-3-methyl-1-tributylstannyl-1-butene, 0.04 gram of tri-2-furylphosphine, 0.04 gram of tris(dibenzylidineacetone)dipalladium(0) in about 30 mL of N,N-dimethylformamide, yielding 2,4-diamino-6-methyl-5-[1-fluoro-3-methyl-3-(4-chlorophenyl)-1-butenyl]pyrimidine.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05622954uspto-grants-1997_04